A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv951108



Internal ID16953295
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr8:15559192..15579191hg38UCSC Ensembl
Outerchr8:15416701..15436700hg19UCSC Ensembl
Cytoband8p22
Allele length
AssemblyAllele length
hg3820000
hg1920000
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2998702
SamplesBILGI_BIOE
Known GenesTUSC3
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nsv951108
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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